237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,347 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
RYBP · rs7652333
See detailed info → StandardZNF831 · rs78302204
See detailed info → StandardRP11-542A14.1 · rs7442660
See detailed info → StandardKDM2B · rs10444491
See detailed info → StandardGUCY1A3 · rs7688323
See detailed info → StandardCREB3L1 · rs72910057
See detailed info → StandardMECOM · rs2421647
See detailed info → StandardWT1 · rs7110547
See detailed info → StandardAC016725.4 · rs12463645
See detailed info → StandardZEB2 · rs7599224
See detailed info → StandardVDR · rs117913411
See detailed info → StandardSLC7A1 · rs866573
See detailed info → StandardSPI1 · rs12801188
See detailed info → StandardCMIP · rs62046579
See detailed info → StandardRP4-663N10.1 · rs12058002
See detailed info → StandardEBF1 · rs36071027
See detailed info → StandardALDOA · rs9939774
See detailed info → StandardAC007092.1 · rs1861410
See detailed info → StandardVGLL4 · rs1000010
See detailed info → StandardENPEP · rs139051778
See detailed info →Showing 20 of 237 · page 4 of 12
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.